电解质
枝晶(数学)
膜
材料科学
锂(药物)
化学工程
金属锂
聚烯烃
分离器(采油)
电化学
金属
多收费
离子电导率
纳米技术
极化(电化学)
纳米纤维
热稳定性
多孔性
阴极
聚丙烯腈
电导率
过电位
锂电池
静电纺丝
无机化学
表面改性
离子液体
电镀(地质)
溶解
电流密度
制作
阳极
电极
作者
Arshad Hussain,M. Hossain,Muhammad Faheem,Yuda Prima Hardianto,Hilal Ahmad,Turki N. Baroud,Md. Abdul Aziz
出处
期刊:
[American Chemical Society]
日期:2025-10-18
卷期号:3 (11): 3812-3824
标识
DOI:10.1021/acsaenm.5c00558
摘要
The uncontrolled growth of lithium dendrites on the anode and the inadequate thermal stability of the present polyolefin separators diminish the electrochemical performance and safety of lithium batteries (LBs). This study involved the fabrication and comprehensive characterization of electrospun PVDF-HFP/MXene nanofiber membranes, focusing on the shape, crystallinity, porosity, electrolyte absorption, and electrochemical characteristics. The prepared membrane functions in a saturated liquid electrolyte environment (1 M LiPF6 in EC/DMC, 1:1 v/v), where its porous architecture and surface chemistry facilitate elevated electrolyte affinity (480%) and ionic conductivity (2.02 mS cm–1). In symmetric Li/Li cells, the PVDF-HFP/MXene separator exhibits stable cycling with diminished polarization for 350 h at a high current density of 1.5 mA cm–2, and postmortem SEM surface and cross-sectional analyses validate more uniform lithium deposition and inhibited dendrite growth. In complete LiFePO4/Li cells, the membrane demonstrates exceptional cycling stability after 300 cycles and a superior rate capability. The findings underscore the promise of PVDF-HFP/MXene membranes as secure and high-performance separators for lithium batteries.
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